Department of Psychology, Marquette University, Milwaukee, Wisconsin.
Department of Psychology, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin.
Biol Psychiatry Cogn Neurosci Neuroimaging. 2022 Feb;7(2):139-149. doi: 10.1016/j.bpsc.2021.08.007. Epub 2021 Sep 1.
Posttraumatic stress disorder (PTSD) is a debilitating disorder, and there is no current accurate prediction of who develops it after trauma. Neurobiologically, individuals with chronic PTSD exhibit aberrant resting-state functional connectivity (rsFC) between the hippocampus and other brain regions (e.g., amygdala, prefrontal cortex, posterior cingulate), and these aberrations correlate with severity of illness. Previous small-scale research (n < 25) has also shown that hippocampal rsFC measured acutely after trauma is predictive of future severity using a region-of-interest-based approach. While this is a promising biomarker, to date, no study has used a data-driven approach to test whole-brain hippocampal FC patterns in forecasting the development of PTSD symptoms.
A total of 98 adults at risk of PTSD were recruited from the emergency department after traumatic injury and completed resting-state functional magnetic resonance imaging (8 min) within 1 month; 6 months later, they completed the Clinician-Administered PTSD Scale for DSM-5 for assessment of PTSD symptom severity. Whole-brain rsFC values with bilateral hippocampi were extracted (using CONN) and used in a machine learning kernel ridge regression analysis (PRoNTo); a k-folds (k = 10) and 70/30 testing versus training split approach were used for cross-validation (1000 iterations to bootstrap confidence intervals for significance values).
Acute hippocampal rsFC significantly predicted Clinician-Administered PTSD Scale for DSM-5 scores at 6 months (r = 0.30, p = .006; mean squared error = 120.58, p = .006; R = 0.09, p = .025). In post hoc analyses, hippocampal rsFC remained significant after controlling for demographics, PTSD symptoms at baseline, and depression, anxiety, and stress severity at 6 months (B = 0.59, SE = 0.20, p = .003).
Findings suggest that functional connectivity of the hippocampus across the brain acutely after traumatic injury is associated with prospective PTSD symptom severity.
创伤后应激障碍(PTSD)是一种使人虚弱的疾病,目前尚无准确预测谁会在创伤后患上这种疾病的方法。从神经生物学角度来看,患有慢性 PTSD 的个体在海马体和其他大脑区域(如杏仁核、前额叶皮层、后扣带回)之间表现出异常的静息态功能连接(rsFC),并且这些异常与疾病的严重程度相关。以前的小规模研究(n<25)还表明,使用基于感兴趣区域的方法,创伤后急性测量的海马体 rsFC 可预测未来的严重程度。虽然这是一种很有前途的生物标志物,但迄今为止,还没有研究使用数据驱动的方法来测试全脑海马体 FC 模式,以预测 PTSD 症状的发展。
共有 98 名有 PTSD 风险的成年人在创伤后从急诊室招募,并在 1 个月内完成静息态功能磁共振成像(8 分钟);6 个月后,他们完成了用于评估 PTSD 症状严重程度的 DSM-5 临床医生管理 PTSD 量表。使用 CONN 提取双侧海马体的全脑 rsFC 值,并在机器学习核脊回归分析(PRoNTo)中使用;使用 k-折交叉验证(k=10)和 70/30 测试与训练分割方法(进行 1000 次迭代以引导置信区间以确定显著性值)。
急性海马体 rsFC 显著预测了 6 个月时的 DSM-5 临床医生管理 PTSD 量表评分(r=0.30,p=0.006;均方误差=120.58,p=0.006;R=0.09,p=0.025)。在事后分析中,在控制人口统计学、基线时的 PTSD 症状以及 6 个月时的抑郁、焦虑和压力严重程度后,海马体 rsFC 仍然显著(B=0.59,SE=0.20,p=0.003)。
研究结果表明,创伤后急性时大脑中海马体的功能连接与前瞻性 PTSD 症状严重程度有关。